Hello readers! This is Verena writing again. This is something I wrote a few days ago. I like to write my thoughts on paper. I don’t share this to get pity; I share this as I know many of you may find this encouraging or many of you may want to understand how muscular dystrophy works.
As a child, I saw people in wheelchairs, power chairs, mobility scooters, and many other equipment. Also, people who use walkers, canes and so many other different types of equipment to make their everyday life easier. I never once thought I would need to rely on any of those.
At the age of 11, I was diagnosed with Limb-girdle type 2A muscular dystrophy after many falls that led to a brain injury. I didn’t understand what a huge effect muscular dystrophy would have in my life. How much of my abilities it would take from me. I didn’t understand what those words really meant.
Muscular dystrophy didn’t progress too quickly on me, which I can be thankful for. Once I was 25 years old, I depended on my cane a lot. The cane was my best friend; I could get around better outside with it. When I fell, I could use my cane to get up. Walking became harder and harder. Just a small distance seemed to take all my effort. I fell way too often, hurt myself way too much. I finally accepted the fact that I would no longer be able to walk at the age of 26 1/2.
I am now 28 years old, and I can’t go without my mobility scooter. My scooter is my legs, my way of getting around on my own, my independence. Being confined to a scooter has many trials. I never realize how much I use my scooter until it quits working. I feel so helpless and discouraged every time it happens.
Limb-girdle type 2A Muscular Dystrophy can feel very cruel. The weakness of the muscles doesn’t just quit when it gets to a certain stage. The weakness continues to get worse year after year. It’s not something you can just accept one time. It’s something you have to accept over and over again. It takes away your running, jumping, biking, and many activities that you love to do. Before you know it, you can’t get off the floor on your own. You can’t climb the stairs anymore. It goes on and on. It affects the muscles around your shoulders, upper limbs, hips, and thighs. It makes the simple things hard to do. Such as lifting your arms, getting up from a chair, and many other things that should be simple.
Muscular dystrophy can take many things from me, but it will not take away my happiness, nor will it take away my faith. This disease is a God-given thing. Although we can’t always understand what he has in store for us, we can always know he makes no mistakes. There’s a purpose for each one of us here on this earth. I will never give up and will not let this disease control me. Each one of us has the opportunity to make our own choices. I choose to never let muscular dystrophy define who I am. The upkeep with the mobility scooter, the doctor visits, and so many things that come with muscular dystrophy. It does get costly at times, but I think we can all say we go through things that cost us a lot. We all have struggles in our life, whether they are visible or not.
I discovered writing my feelings and my thoughts on a paper helps me a lot. I don’t always like to cry about my problems to my loved ones as they have struggles too. Although I often do and they are always willing to listen. I have 3 other siblings with this disease as well.
That’s some of my story, and I’m forever grateful for my husband, my family, his family, friends, and to my heavenly Father. Without them, this disease would be much harder.
God Bless!
OVEN-ROASTED POTATOES
2 pounds red potatoes
1/4 cup olive oil
Sprinkle with seasoning of your choice (I have used seasoning salt, lemon pepper, garlic seasoning or ranch seasoning)
Preheat the oven to 450 degrees. Place potatoes in a 1-gallon-size zipper bag and add oil; seal bag. Toss to coat. Add seasoning and toss again until coated. Bake in an ungreased baking sheet for 30 to 35 minutes or until potatoes are brown and crisp
Lovina’s Amish Kitchen is written by Lovina Eicher, Old Order Amish writer, cook, wife, and mother of eight. Her three cookbooks, The Cherished Table, The Essential Amish Cookbook, and Amish Family Recipes, are available wherever books are sold. Readers can write to Eicher at Lovina’s Amish Kitchen, PO Box 234, Sturgis, MI 49091 (please include a self-addressed stamped envelope for a reply); or email questionsforlovina@gmail.com and your message will be passed on to her to read. She does not personally respond to emails.

Verena, your column about your muscular dystrophy is a very powerful testimony. Thank you for sharing.
I enjoy reading this column every week. May God bless as you travel the road he has for you.
Thank you for your valuable post. So informative. My prayers are with you.
Thank you, Verena, for sharing more about yourself. Faith, family and friends do make our challenges easier. It is always good to hear from you. Keep writing.
Wonderful article! Your positivity is the best! Blessings to you and all of your family.
Hi Verena,
Just read your column today. I was so glad you shared your experience with your disability with us. It certainly gave me an insight into what your day is like. I admire your ability to accept your limitations but work with what you have and move forward. You definitely have an attitude of gratitude. I work towards that everyday.
Blessings for you and all your family.
judy
Thank you for sharing about your troubles Verena, yes God is our hope and help every day, blessings.
Verena, I so enjoyed your column. It makes me realize how much we take for granted, and still complain. It is a real wake-up call.
I pray for you and your families and admire all the challenges you cope with every day.
Take care.
Thank you for sharing. I have a friend who has Muscular Sclerosis (MS) and her attitude is much like yours.
You might want to add in your recipe instructions to take the oiled and seasoned potatoes out of the plastic bag before baking!
Thankyou for sharing. All of us have struggles but stating positive is the key. Blessings
I read this column faithfully. Your attitude is amazing. I do know that with God anything is possible. Thank you for sharing about your life and giving an understanding about muscular dystrophy . May the Lord bless you.
God Bless YOU and your beloved family, Verena. You are an inspiration and I know that in your sharing the hardship of this disease and yet your exceptional attitude of gratefulness and clarity of God’s hand in your life, you will change other’s lives. I will pray and think of you often.
Verena, thank you for your column today sharing insights into living with muscular dystrophy. I appreciate your “can do with God’s help”, never give up or in attitude. Please continue to stay positive even though the road gets hard sometimes. God bless you and your family!
Verna,
You are a strong woman to have the health problem that you do and can still find the good things in life to praise God for!
I enjoyed your story & hope your health permits you to continue in your mother’s shadow and continue to help her with the column she writes each month. May God Bless you all!